Element for electrophoresis

BACKGROUND OF THE INVENTION

1. Field of the invention

This invention relates to an element for electrophoresis, and more particularly relates to an element for electrophoresis suitably employable for electrophoresis of biopolymers such as proteins.

2. Description of prior arts

The electrophoresis can be carried out in the following manner: a membrane medium for electrophoresis prepared by coating or casting a membrane-forming material such as agar, cellulose, cellulose acetate, starch, silica gel or polyacrylamide gel over a support such as a glass plate or transparent plastic sheet (or film) is impregnated with a buffer solution; on the medium is applied a substance to be analyzed (sample); the applied sample is developed (or resolved) on or in the medium by applying a voltage between the both ends of the support and dyed thereon; and then the dyed sample is measured on the optical density to quantitatively determine the components of the sample.

Details of the electrophoresis and medium therefor are given in "Experimental Text for Electrophoresis (5th revision)" editted by Electrophoresis Society of Japan (Bunkodo, 1975), "Modern Electrophoresis" editted by Aoki & Nagai (Hirokawa Shoten, 1973), etc.

Recently, the electrophoresis has been employed to analyze substances originating from a living body; for instance, the analyses of proteins originating from a living body are generally performed in the course of biochemical analysis for diagnosis.

As the membrane or sheet for electrophoresis, a filter paper was previously employed, but recently an agarose membrane or a polyacrylamide gel membrane (or medium) has been employed from the viewpoints of their advantageous properties. Particularly, the polyacrylamide gel membrane showing melecular sieve function is widely employed recently. The polyacrylamide gel membrane can be prepared by crosslinking polymerization of a monomer such as acrylamide and a two-functional crosslinking agent such as N,N'-methylenebisacrylamide under an oxygen-free condition in the presence of water and a polymerization catalyst.

In the course of the preparation of the polyacrylamide gel membrane, a modifier such as an anionic surfactant is incorporated into the membrane in certain cases. Since only a small amount of the modifier is required for the preparation of the gel membrane for protein analysis, the modifier can be incorporated into the membrane by applying an aqueous modifier solution onto the wet gel membrane or immersing the gel membrane in an aqueous modifier solution.

Since the polymerization reaction for the preparation of polyacrylamide is a radical crosslinking polymerization as described above, the polymerization can be easily inhibited by the presence of oxygen. Therefore, the gel membrane should be prepared in the absence of oxygen. For this reason, a polyacrylamide gel membrane is generally prepared by a process involving: introducing an aqueous solution (gel-forming solution or gel solution) containing acrylamide, a crosslinking agent and a polymerization catalyst into a cell formed between two glass plates with a certain clearance (e.g., 0.3-1 mm); sealing the gel-forming solution from oxygen; and causing the crosslinking polymerization to prepare the desired gel membrane. This procedure employing glass plates are disadvantageous because the glass plate is easily breakable and rather heavy and careful handling is accordingly required. Thus, the above procedure employing the glass plates is difficultly utilized to prepare the polyacrylamide gel membrane in a mass scale.

For the reasons described above, it has been desired that the the glass plate for supporting the polyacrylamide gel membrane is replaced with a light-weight plastic material support. However, for the use of a satisfactorily acceptable plastic material support such as a polyethylene terephthalate (PET) sheet, poor adhesion between the gel membrane and the plastic material support should be improved, for the reasons given below.

The prepared polyacrylamide gel is horizontally or vertically placed for performing slab electrophoresis. The electrophoresis is performed for a certain period of time under predetermined conditions, and the desired analysis of the components originating from the living body is done after dyeing the electrophoresed gel membrane with Ponceau 3R (Ciba-Geigy), Coomassie Brilliant Blue G-250 (ICI), silver, etc. The gel membrane is apt to separate from the support in the dyeing procedure even in the case of employing the glass plate support. Accordingly, the dyeing procedure requires highly skilled operation to prevent the separation of the gel membrane from the support. The poor affinity of the plastic material support to the polyacrylamide gel membrane makes it more difficult to handle the element for electrophoresis without separation of the support from the gel membrane.

SUMMARY OF THE INVENTION

An object of the present invention is to provide a element for electrophoresis which is improved in the adhesion between the support and the polyacrylamide gel medium such as in the form of a membrane.

Another object of the present invention is to provide a element for electrophoresis which is substantially free from separation between the polyacrylamide gel medium and the support in the course of a dyeing stage and a subsequent drying stage.

There is provided by the present invention a element for electrophoresis comprising the following three-layer structure laminated in the order:

(I) a support layer;

(II) an adhesive layer comprising a polymer having at least one repeating unit selected from the group consisting of:

(1) a repeating unit having the formula (1): ##STR1## in which R¹¹ is the hydrogen atom or an alkyl group containing 1-6 carbon atoms; Q¹ is --COO--, --CON(R¹¹)--, or an arylene group containing 6-10 carbon atoms; L¹ is a divalent group containing at least one linkage selected from the group consisting of --COO-- and --CON(R¹¹)-- and containing 3-15 carbon atoms, or a divalent atom containing at least one linkage selected from the group consisting of --O--, --N(R¹¹)--, --CO--, --SO--, --SO₂ --, --SO₃ --, --SO₂ N(R¹¹)--, --N(R¹¹)CON(R¹¹) and --N(R¹¹)COO--, and containing 1-12 carbon atoms, in which R¹¹ has the same meaning as defined above; R¹² is --CH═CH₂ or --CH₂ CH₂ X¹, in which X¹ is a substituent replaceable with a nucleophilic group or releasable in the form of HX¹ by a base; and x¹ and y¹ both representing molar percents range from 0 to 99 and from 1 to 100, respectively, and x¹ +y¹ is not less than 90;

(2) a repeating unit having the formula (2): ##STR2## in which R²¹ is the hydrogen atom or an alkyl group containing 1-6 carbon atoms; R²² is --CH═CH₂ or --CH₂ CH₂ X², in which X² is a substituent replaceable with a nucleophilic group or releasable in the form of HX² by a base; L² is a divalent group selected from the group consisting of an alkylene group containing 1-6 carbon atoms, an arylene group containing 6-12 carbon atoms, --COZ² --, and --COZ² R²³ --, in which R²³ is an alkylene group containing 1-6 carbon atoms, or an arylene group containing 6-12 carbon atoms, and Z² is the oxygen atom or NH; and x² and y² both representing molar percents range from 10 to 95 and from 5 to 90, respectively, and x² +y² is not less than 90; and

(3) a repeating unit having the formula (3): ##STR3## in which R³¹ is the hydrogen atom or an alkyl group containing 1-6 carbon atoms; L³ is a divalent linkage group containing 1-20 carbon atoms; X³ is an active ester; x³ and y³ both representing molar percent range from 0 to 95 and from 5 to 100, respectively, and x³ +y³ is not less than 90; and m is 0 or 1;

and

(III) a medium layer for electrophoresis comprising an aqueous polyacrylamide gel formed by crosslinking polymerization of an acrylamide compound and a crosslinking agent in the presence of water.

The element for electrophoresis of the present invention comprises a three-layer structure in which the support layer and the medium layer are combined by means of the specific adhesive layer. This three-layer structure is hardly separated in the course of a variety of operations performed in the aforementioned dyeing stage. Accordingly, the element for electrophoresis of the present invention is very advantageous for performing the electrophoresis process.

Moreover, the element for electrophoresis of the present invention can be prepared by forming the adhesive layer on a horizontally placed support and subsequetnly forming the medium layer thereon. Therefore, the element for electrophoresis of the invention is advantageously prepared in a mass scale.

DETAILED DESCRIPTION OF THE INVENTION

Examples of the support employable for the preparation of the element for electrophoresis of the present invention include glass plate, paper sheet and a variety of plastic material sheets. The support of plastic material sheet is preferably employed to effectively utilize the advantageous feature of the present invention. The plastic material sheet can be made of an optionally selected material, but a polyethylene terephthalate sheet is preferably employed.

Description of the adhesive layer

According to the present invention, an adhesive layer is provided on the support.

The adhesive layer comprises a polymer having at least one repeating unit selected from the group consisting of the following repeating units represented by the formulae (1), (2) and (3).

(1) A repeating unit having the formula (1): ##STR4## in which R¹¹ is the hydrogen atom or an alkyl group containing 1-6 carbon atoms; Q¹ is --COO--, --CON(R¹¹)--, or an arylene group containing 6-10 carbon atoms; L¹ is a divalent group containing at least one linkage selected from the group consisting of --COO-- and --CON(R¹¹)-- and containing 3-15 carbon atoms, or a divalent atom containing at least one linkage selected from the group consisting of --O--, --N(R¹¹)--, --CO--, --SO--, --SO₂ --, --SO₃ --, --SO₂ N(R¹¹)--, --N(R¹¹)CON(R¹¹) and --N(R¹¹)COO--, and containing 1-12 carbon atoms, in which R¹¹ has the same meaning as defined above; R¹² is --CH═CH₂ or --CH₂ CH₂ X¹, in which X¹ is a substituent replaceable with a nucleophilic group or releasable in the form of HX¹ by a base; and x¹ and y¹ both representing molar percents range from 0 to 99 and 1 to 100, preferably from 50 to 95 and from 5 to 50, respectively, and x¹ +y¹ is not less than 90, preferably not less than 95, most preferably 100.

Examples of R¹¹ in the above formula (1) include methyl, ethyl, butyl and n-hexyl groups.

Examples of Q¹ include ##STR5##

Examples of L¹ include the following divalent groups, which can be arranged in any direction within the formula (1), so far as it can connect Q¹ and SO₂ :

--CH₂ COOCH₂ --, --CH₂ COOCH₂ CH₂ --, --CH₂ CH₂ COOCH₂ --, --(CH₂)₅ COOCH₂ CH₂ --, --(CH₂)₁₀ COOCH₂ CH₂ --, --CH₂ NHCOCH₂ --, --CH₂ NHCOCH₂ CH₂ --, --(CH₂)₃ NHCOCH₂ CH₂ --, --(CH₂)₅ NHCOCH₂ CH₂ --, --(CH₂)₁₀ NHCOCH₂ CH₂ --, --CH₂ OCH₂ --, --CH₂ CH₂ OCH₂ CH₂ CH₂ --, --N(CH₃)CH₂ CH₂ --, --CH₂ N(CH₃)CH₂ CH₂ -- --COCH₂ CH₂ --, --CH₂ COCH₂ CH₂ --, ##STR6## --SOCH₂ CH₂ --, --CH₂ SOCH₂ CH₂ --, --SO₂ CH₂ CH₂ --, --SO₂ CH₂ CH₂ SO₂ CH₂ CH₂ --, --SO₂ CH₂ CH₂ SO₂ CH₂ CH(OH)CH₂ --, --SO₃ CH₂ CH₂ CH₂ --, --SO₃ CH₂ COOCH₂ CH₂ --, --SO₃ CH₂ CH₂ COOCH₂ CH₂ --, --SO₃ CH₂ CH₂ CH₂ --, --SO₂ NHCH₂ COOCH₂ CH₂ --, --SO₂ NHCH₂ CH₂ COOCH₂ CH₂ --, --NHCONHCH₂ CH₂ --, --CH₂ NHCONHCH₂ CH₂ --, --NHCOOCH₂ CH₂ --, and --CH₂ NHCOOCH₂ CH₂ --.

R¹² is --CH═CH₂ or --CH₂ CH₂ X¹. Examples of X¹ include:

halogen atoms such as chlorine and bromine;

hydroxyl group;

alkylsulfonyloxy groups such as methylsulfonyloxy (H₃ CSO₃ --), ethylsulfonyloxy, and propylsulfonyloxy;

arylsulfonyloxy groups such as phenylsulfonyloxy ##STR7## and p-tolylsulfonyloxy; and alkylcarbonyloxy groups such as acetoxy, propionyloxy, trifluoromethylcarbonyloxy and dichloromethylcarbonyloxy. Accordingly, examples of R¹² include the following groups: ##STR8##

(2) A repeating unit having the formula (2): ##STR9## in which:

R²¹ is the hydrogen atom or an alkyl group containing 1-6 carbon atoms;

R²² is --CH═CH₂ or --CH₂ CH₂ X², in which X² is a substituent replaceable with a nucleophilic group or releasable in the form of HX² by a base;

L² is a divalent group selected from the group consisting of an alkylene group containing 1-6 carbon atoms (e.g., methylene, ethylene or isobutylene), an arylene group containing 6-12 carbon atoms (e.g., phenylene, tolylene or naphthalene), a group represented by --COZ² --, and a group represented by --COZ² R²³ --, in which R²³ is an alkylene group containing 1-6 carbon atoms, or an arylene group containing 6-12 carbon atoms, and Z² is the oxygen atom or NH; and

x² and y² both representing molar percents range from 10 to 95 and from 5 to 90, preferably from 50 to 95 and from 5 to 50, respectively, and x² +y² is not less than 90, preferably not less than 95, most preferably 100.

In the formula (2), examples of R²¹ and R²² include the respective groups listed for R¹¹ and R¹² of the formula (1).

(3) A repeating unit having the formula (3): ##STR10## in which:

R³¹ is the hydrogen atom or an alkyl group containing 1-6 carbon atoms;

L³ is a divalent linkage group containing 1-20 carbon atoms, preferably a divalent group containing 1-12 carbon atoms having --CONH-- or --CO-- linkage therein;

X³ is an active ester;

x³ and y³ both representing molar percent range from 0 to 95 and from 5 to 100, preferably from 50 to 95 and from 5 to 50, respectively, and x³ +y³ is not less than 90, preferably not less than 95, most preferably 100; and

m is 0 or 1.

In the formula (3), examples of R³¹ include the groups listed for R¹¹ of the formula (1).

Examples of L³ include the following groups:

--COCH₂ --, --COCH₂ CH₂ OCOCH₂ CH₂ --, --CONHCH₂ --, --CONHCH₂ CH₂ --, --CONHCH₂ CH₂ CH₂ --, --CONHCH₂ CH₂ CH₂ CH₂ --, --CONHCH₂ CONHCH₂ --, --CONHCH₂ CONHCH₂ CONHCH₂ --, --CONHCH₂ NHCOCH₂ CH₂ CH₂ SCH₂ CH₂ --, and --CONHCH₂ OCOCH₂ CH₂ --.

Examples of X³ include the following groups: ##STR11##

Processes for syntheses of representative ethylenic unsaturated monomers containing a vinylsulfonyl groups or a functional group convertible into a vinylsulfonyl group which are employable for the preparation of the polymers comprising the repeating unit represented by the formula (1), (2) or (3) are illustrated below.

SYNTHESIS EXAMPLE 1

Synthesis of 2-[3-(2-chloroethylsulfonyl)propionyloxy]ethyl acrylate

<pre xml:space="preserve" listing-type="equation"> <!--Greenbook equation-->CH₂ ═CHCOOCH₂ CH₂ OCOCH₂ CH₂ SO₂ CH₂ CH₂ Cl</pre>

Into a mixture of 600 ml. of tetrahydrofuran, 45.8 g. of hydroxyethyl acrylate, and 72 g. of 3-(2-chloroethylsulfonyl)propionyl chloride placed in a reaction vessel chilled with ice-water to maintain the temperature below 5° C., a solution of 31.2 g. of pyridine in 100 ml. of tetrahydrofuran was poured dropwise for 1.75 hours. The resulting mixture was stirred at room temperature for 2 hours, and poured into 2.5 l. of ice-water. The aqueous mixture was then extracted with 4 portions of 300 ml. of chloroform. The organic extract was dried over sodium sulfate, and concentrated to give 87 g. of 2-[3-(2-chloroethylsulfonyl)propionyloxy]ethyl acrylate (yield 88%).

SYNTHESIS EXAMPLE 2

Synthesis of N-[3-(2-chloroethylsulfonyl)propanamidomethyl]acrylamide

<pre xml:space="preserve" listing-type="equation"> <!--Greenbook equation-->CH₂ ═CHCONHCH₂ NHCOCH₂ CH₂ SO₂ CH₂ CH₂ Cl</pre>

In a 2-l. reaction vessel, 1,400 ml. of distilled water, 244 g. of sodium sulfite and 220 g. of sodium hydrogencarbonate were stirred to give a solution. To the resulting solution chilled with ice-water to maintain the temperature at approx. 5° C. was dropwise added for 1.5 hours 260 g. of chloroethanesulfonyl chloride. To the resulting mixture was further added dropwise for approx. 15 min. 160 g. of 49% sulfuric acid. The mixture was then stirred at 5° C. for 1 hour, and the produced crystalline precipitate was filtered off. The precipitate was then washed with 400 ml. of distilled water. The filtrate and the water collected from the washing were together introduced into a 3-l. reaction vessel. Into the reaction vessel chilled with ice to maintain the temperature at approx. 5° C. was dropwise added for 30 min. a solution of 246 g. of methylenebisacrylamide in a mixture of 480 ml. of distilled water and 1,480 ml of ethanol. The reaction vessel was then stored in a refrigerator for 5 days to complete the reaction. The precipitated crystals were collected by filtration and washed with 800 ml. of chilled distilled water. The crystals were then recrystallized from 2,000 ml. of 50% aqueous ethanol to give 219 g. of the desired monomer: yield 49%. Analysis: H 5.17%; C 37.90%; N 9.48%; Cl 12.58%.

SYNTHESIS EXAMPLE 3

Synthesis of {[3-(2-chloroethylsulfonyl)propanamido]methyl}styrene ##STR12##

Into a mixture of 100 ml. of tetrahydrofuran, 20.1 g. of vinylbenzylamine, 16.7 g. of triethylamine, and 0.1 g. of hydroquinone placed in a reaction vessel chilled with ice-water a solution of 36.1 g. of β-chloroethylsulfonylpropionyl chloride in 200 ml. of tetrahydrofuran was poured dropwise for 30 min. The resulting mixture was allowed to stand overnight at room temperature. Subsequently, the mixture was poured into a diluted sulfuric acid prepared from 16.5 g. of conc. sulfuric acid and 1.5 l. of ice-water. The produced precipitate was collected by filtration. The collected precipitate was recrystallized from a mixture of 200 ml. of ethanol and 200 ml. of water to give 26.8 g. of {[3-(2-chloroethylsulfonyl)propanamido]methyl}styrene: yield 57%. Analysis: H 5.74%; C 53.47%; N 4.83%; Cl 10.99%; S 10.49%.

SYNTHESIS EXAMPLE 4

Synthesis of 1-[2-(4-vinylphenylsulfonyl)ethylsulfonyl]-3-(2-chloroethyl)sulfonyl-2-propanol ##STR13##

To a mixture of 157 g. of 1,3-bis(2-chloroethyl)sulfonyl-2-propanol (prepared by the method disclosed in Japanese Patent Provisional Publication No. 53(1978)57257), 1 l. of methanol and 1 l. of distilled water placed in a reaction vessel and heated to 46° C. was dropwise added for 1 hour a solution of 52 g. of potassium vinylbenzenesulfinate in a mixture of 100 ml. of methanol and 100 ml. of distilled water. The resulting mixture was further stirred at 46° C. for 5.5 hours. The produced precipitate was collected to give 55 g. of 1-[2-(4-vinylphenylsulfonyl)ethylsulfonyl]-3-(2-chloroethyl)sulfonyl-2-propanol: yield 49%. Analysis: H 4.67%; C 39.89%; S 21.43%.

Among the polymers defined hereinbefore, polymers comprising the following repeating unit are preferred for the polymer employed for the formation of the adhesive layer according to the present invention. ##STR14##

In the above formula, the numerals outside of the brackets indicate mole percents, and R means the following substitutent.

<pre xml:space="preserve" listing-type="tabular"> <!--Greenbook tabular data-->______________________________________P-1 COOCH₂ CH₂ OCOCH₂ CH₂ SO₂ CHCH₂P-2 CONHCH₂ NHCOCH₂ CH₂ SO₂ CHCH₂P-3 ##STR15##P-4 COOCH₂ CH₂ OCOCH₂ SO₂ CH₂ CH₂ ClP-5 CONHCH₂ NHCOCH₂ CH₂ SO₂ CH₂ CH₂ ClP-6 ##STR16##P-7 ##STR17##______________________________________</pre>

Processes for the synthesis of the preferable polymer having the above-mentioned repeating unit in which R is P-1, P-2 or P-5 are illustrated below.

SYNTHESIS EXAMPLE 5

Synthesis of copolymer of 2-[3-(vinylsulfonyl)propionyloxy]ethyl acrylate and acrylamide (corresponding to P-1)

In a reaction vessel, a mixture of 60 ml. of N,N-dimethylformamide, 14.5 g. of 2-[3-(2-chloroethylsulfonyl)propionyloxy]ethyl acrylate, and 32.6 g. of acrylamide was purged by nitrogen gas and heated to 60° C. To the heated mixture was added 0.40 g. of 2,2'-azobis(2,4-dimethylvaleronitrile)[CAS Registry No. 4419-11-8], and the resulting mixture was heated under stirring for 2 hours. Subsequently, 0.20 g. of 2,2'-azobis(2,4-dimethylvaleronitrile) was added to the mixture, and the resulting mixture was further heated under stirring for 2 hours. The mixture was then chilled to 5° C., and after addition of 12 g. of sodium carbonate and 4.9 g. of triethylamine, stirred for one hour. The mixture was then stirred at room temperature for 1 hour. This was introduced into a cellulose tube and subjected to dialysis for 2 days. The remaining solid was freeze-dried to give 43 g. of white polymer: yield 95%.

The vinylsulfonyl content of thus obtained polymer was 1.0×10^-3 eq./g.

SYNTHESIS EXAMPLE 6

Synthesis of copolymer of N-{[3-(vinylsulfonyl)propanamido]methyl}acrylamide and acrylamide (corresponding to P-2)

In a 200-ml. reaction vessel, 5.65 g. of the monomer of the synthesis example 2, 12.8 g. of acrylamide, and 80 ml. of 50% aqueous methanol were heated to 60° C. under stirring. To the resulting mixture was added 0.1 g. of 2,2'-azobis(2,4-dimethylvaleronitrile) and after 30 min. further added 0.1 of the same reagent. The mixture was then heated under stirring for 1 hour, and chilled with ice-water to approx. 10° C. To the chilled mixture was added a solution of 2.5 g. of triethylamine in 80 ml. of methanol, and the mixture was further stirred. The mixture was then added under stirring to 1 l. of acetone. The produced precipitate was collected by filtration to give 15.9 g. of the desired polymer: yield 90%.

The sulfonyl content of thus obtained polymer was 0.95×10^-3 eq./g.

SYNTHESIS EXAMPLE 7

Synthesis of copolymer of N-{[3-(2-chloroethylsulfonyl)propanamido]methyl}acrylamide and acrylamide (corresponding to P-5)

In a 500-ml. reaction vessel, 10.3 g. of the monomer of the synthesis example 2, 15.6 g. of acrylamide, and 160 ml. of 50% aqueous methanol were heated to 60° C. under stirring. To the resulting mixture was added 0.2 g. of 2,2'-azobis(2,4-dimethylvaleronitrile) and after 30 min. further added 0.2 g. of the same reagent. The mixture was then heated under stirring for 1 hour. This was introduced into a cellulose tube and subjected to dialysis for 2 days. The remaining solid was freeze-dried to give 23 g. of white polymer: yield 90%.

The chlorosulfonyl content of thus obtained polymer was 1.0×10^-3 eq./g.

The adhesive layer comprises the copolymer defined as above, and can be formed on a surface of the support in the conventional manner. In the case that the copolymer is water-soluble or hydrophilic, an aqueous solution thereof or a solution thereof in a mixture of water and an organic solvent may be coated over the surface and dried in a conventional manner to form the adhesive layer. In the case that the copolymer is hydrophobic and water-insoluble, a solution thereof in an organic solvent or a mixture of an organic solvent and a small amount of water may be coated over the surface and dried in a conventional manner to form the adhesive layer.

Examples of the organic solvent employable in the above-mentioned procedure include ketones such as acetone and methyl ethyl ketone; alcohols such as methanol and ethanol; N,N-dimethylformamide; dimethylsulfoxide; and ethers such as dimethyl ether and dioxane.

The thickness of the adhesive layer after dryness ranges from approx. 0.1 μm to approx. 3 μm, preferably from approx. 0.2 μm to approx. 2 μm.

Description on the medium for electrophoresis (polyacrylamide gel membrane)

For the preparation of the polyacrylamide gel membrane, an acrylamide compound and a crosslinking agent are dissolved or dispersed in water to prepare an aqueous solution or an aqueous dispersion, in which the crosslinking reaction is carried out to form an aqueous polyacrylamide gel membrane. Hereinafter, the term "dissolving (in water)" means to include both "dissolving (in water)" and "dispersing (in water)", and the term "aqueous solution" means to include both "aqueous solution" and "aqueous dispersion", unless otherwise indicated. The term "aqueous medium" is used to include both a simple water as well as an aqueous mixture of water and an organic solvent, the organic solvent being optionally added.

Examples of the acrylamide compound employable in the present invention include acrylamide and its homologues such a N-methylacrylamide, N,N-dimethylacrylamide, N-(hydroxymethyl)acrylamide and diacetonacrylamide, and these compounds may be employed independently or in combination. Acrylamide is most preferable among these acrylamide compounds, and said acrylamide can be also preferably employed in combination with one or more of other acrylamide compounds.

As the crosslinking agent employable to obtain the polyacrylamide gel membrane of the invention, a known crosslinking agent described, for instance, in "Electrophoresis" 1981, 2, 213-228 can be employed singly or in combination. Examples of the crosslinking agent include bifunctional compounds such as N,N'-methylenebisacrylamide (BIS), N,N'-propylenebisacrylamide (PBA), diacrylamide dimethylether (N,N'-oxydimethyleneacrylamide), 1,2-diacrylamide ethyleneglycol (DEG), 1,3-diacryloylethyleneurea, ethylene diacrylate (EDA), N,N'-diallyltartardiamide (DATD), and N,N'-bisacrylylcystamine (BAC). The crosslinking agent can be employed in the amount of approx. 2 to 30 wt.%, preferably approx. 3 to 10 wt.%, based on the total weight of the monomer (i.e., acrylamide compound) and the crosslinking agent. The gel concentration preferably is in the range of approx. 3 to 30 wt/v % (total weight of monomer and crosslinking agent per total volume of gel membrane comprising monomer, crosslinking agent and aqueous medium), the concentration being in accordance with the definition indicated by S. Hjerten in "Arch. Biochem. Biophys." 1 (Suppl.), 147 (1962).

The element for electrophoresis of the present invention is mainly employed for analysis of proteins and conjugated proteins (e.g., lipoproteins, glycoproteins, etc.) and the medium (gel membrane) of the element may comprise an anionic surfactant as a modifier. The use of the anionic surfactant is generally essential or preferable for the electrophoretic analyses of proteins or conjugated proteins, because it contributes to perform separation of the protein and conjugated protein and determination of molecular weight of these proteins. However, the medium of the element for electrophoresis may not contain the anionic surfactant.

Examples of the anionic surfactant include alkylsulfates, particularly alkylsulfates having a long chain alkyl group of at least 10 carbon atoms. The cation contained for formation of the salt generally is an alkali metal ion such as sodium ion, potassium ion, or lithium ion. Sodium ion is preferred from the economical viewpoint. The alkylsulfates preferably are dodecylsulfates (salts of sodium, potassium, lithium, etc.), and particularly preferred is sodium dodecylsulfate (SDS). The introduction of SDS into the gel membrane is particularly advantageous for separation of proteins and conjugated proteins, as well as for determination of molecular weight thereof. The anionic surfactant (modifier) is contained in the gel-forming solution in the amount of approx. 0.05 to 2.0 wt/v % (weight per volume of the gel-forming solution), preferably approx. 0.1 to 1.5 wt/v %.

The polyacrylamide gel membrane of the invention may contain an oxidation inhibitor. The oxidation inhibitor can be chosen from various compounds heretofore known as oxidation inhibitors employable for the gel membrane for electrophoresis. Examples of the oxidation inhibitor include 1,4-dithiothreitol and 2-mercapto-ethanol.

The polyacrylamide gel membrane of the invention may contain a water-soluble polymer. As the water-soluble polymer, a water-soluble polymer of the addition polymerization type or condensation polymerization type can be used. Examples of the polymer of the addition polymerization type include non-ionic water-soluble polymers such as polyvinyl alcohol, polyvinyl pyrrolidone, and polyacrylamide. Examples of the polymer of the condensation polymerization type include non-ionic water-soluble polyalkylene glycols such as polyethylene glycol and polypropylene glycol. The water-soluble polymer of molecular weight ranging from approx. 10,000 to 1,000,000 is preferably used. Among these water-soluble polymers, polyacrylamide and polyethylene glycol are preferable. The water-soluble polymer is used in a range of approx. 2 to 100 wt.%, preferably, approx. 5 to 50 wt.%, based on the total weight of the monomer and crosslinking agent.

The addition of a water-soluble polymer serves to impart elasticity to the gel membrane, and thus modified gel membrane is still elastic even if it is dried. Thus, the gel membrane is so improved as to be free from the brittleness, whereby the gel membrane becomes hardly breakable. Further, the viscosity of the gel membrane can be controlled by selecting the molecular weight and amount of the water-soluble polymer.

The polyacrylamide gel membrane preferably contain agarose. There is no specific limitation on the agarose to be contained in the gel membrane, and any type of agarose such as low-electroendosmosis agarose, medium-electroendosmosis agarose, or high-electroendosmosis agarose can be used. Examples of agarose employable in the invention include agaroses disclosed in Japanese Patent Provisional Publication Nos. 55(1980)-5730, 55(1980)-110946 (corresponding to U.S. Pat. No. 4,290,911 and GB 2 042 571A), 57(1982)-502098 (WO 82/02599, U.S. Pat. No. 4,319,976), etc. The amount of agarose to be added ranges from approx. 0.2 to 2 wt/v %, preferably from approx. 0.3 to 1.2 wt/v %, based on the volume of the aqueous gel containing the monomer and crosslinking agent. It becomes possible by the addition of agarose that the viscosity of the gel-forming solution can be controlled through changing the temperature of the solution, whereby suppressing flowability of the solution as well as facilitating the formation of the gel membrane.

A pH buffer agent can be contained in the polyacrylamide gel membrane of the invention. Any buffer agent which is able to buffer a solution to a range of pH 2.5 to 10.0 can be used. Buffer agents employable in the invention are described in publications such as "Chemistry Handbook, Fundamental Edition" compiled by The Chemical Society of Japan (Maruzen Ltd., Tokyo, 1966) pages 1312-1320; "Modern Electrophoresis" editted by Aoki &amp; Nagai (Hirokawa Shoten, 1973), pages 320-322; "Data for Biochemical Research" compiled by R. M. C. Dawson et al., second edition (Oxford at the Clarendon Press, 1969) pages 476-508; "Biochemistry" 5, 467 (1966); and "Analytical Biochemistry" 104, pages 300-310 (1966). Examples of the buffer agent include a buffer agent containing barbital, a buffer agent containing tris(hydroxymethyl)aminomethane (Tris), a buffer agent containing phosphate, a buffer agent containing borate, a buffer agent containing acetic acid or acetate, a buffer agent containing citric acid or citrate, a buffer agent containing lactic acid or lactate, and a buffer agent containing glycine; as well as N,N-bis(2-hydroxyethyl)glycine (Bicine), N-2-hydroxyethylpiperazine-N'-2-hydroxypropane-3-sulfonic acid (HEPPSO) or its salt, N-2-hydroxyethylpiperazine-N'-3-propanesulfonic acid (EPPS) or its salt, N-[tris(hydroymethy)methyl]-3-aminopropanesulfonic acid (TAPS) or its salt. Preferable examples of the buffer agent include potassium dihydrogenphosphate-disodium hydrogenphosphate, Tris-sodium borate, Tris-sodium borate-EDTA 2Na, Tris-citric acid, sodium barbital-sodium acetate, sodium barbital-hydrochloric acid, barbital-sodium barbital, acetic acid-sodium acetate, lactic acid-sodium lactate, citric acid-desodium hydrogenphosphate, Bicine, HEPPSO, sodium salt of HEPPSO, EPPS, sodium salt of EPPS, TAPS, sodium salt of TAPS, etc.

The polyacrylamide gel membrane of the element of the invention is formed by radical crosslinking polymerization between the monomer such as acrylamide with the bifunctional compound (crosslinking agent) in an aqueous medium in which the water-soluble polymer and agarose are dissolved almost homogeneously. The gel is assumed to have a structure in which the water-soluble polymer and agarose are dispersed in the three dimensional crosslinked polymer formed by the reaction of the monomer and cross-linking agent, and the water-soluble polymer and agarose dispersed and further entangle with the three dimensional crosslinked polymer structure.

The crosslinking polymerization can be initiated by a known method, for instance, in the presence of a peroxide and/or under irradiation of ultra-violet rays. The reaction can be further accelerated by heat and irradiation with ultra-violet rays.

As the polymerization catalyst, a known low temperature-polymerization initiator such as those described in "Electrophoresis" 1981, 2, 213-219, ibid. 1981, 2, 220-228; and "Modern Electrophoresis" editted by Aoki &amp; Nagai (Hirokawa Shoten, 1973) can be used. Examples of the initiator include a mixture of β-dimethylaminopropionitrile (DMAP) and ammonium peroxodisulfate, a mixture of N,N,N',N'-tetramethylethylenediamine (TEMED) and ammonium peroxodisulfate, a mixture of TEMED and riboflavin, a combination of a mixture of TEMED, riboflavin and hydrogen peroxide, and irradiation with ultra-violet rays. The radical reaction initiator can be employed in the amount of approx. 0.3 to 5 wt. %, preferably approx. 0.5 to 3 wt. %, based on the total amount of the monomer and crosslinking agent.

In the case that the polyacrylamide gel membrane of the element of the invention can be prepared by a process in which a gel forming solution is coated by a known method on an electric insulation support having a smooth hydrophilic surface, and the gel forming solution is crosslinked to polymerization thereon. Some examples of the support are mentioned hereinbefore. In more detail, examples of the support include glass plate, hydrophilic polymers in the form of plate or sheet, and other polymers (e.g., polyethylene terephthalate, polycarbonate of bisphenol A, polyvinyl chloride, vinylidene chloride--vinyl chloride copolymer, polymethylmethacrylate, polyethylene, polypropylne, cellulose acetate, and cellulose acetate propionate) in the form of plate or sheet, a surface of which is made hydrophilic by a known surface treatment. Examples of the treatment employable to make the surface of these polymers hydrophilic include known methods such as irradiation with ultra-violet rays, glow discharge treatment, corona discharge treatment, flame treatment, electron beam treatment, chemical etching, or electrochemical etching. Nevertheless, the hydrophilic surface is not necessarily provided on the support, and the above-mentioned polymer sheet can be employed with no hydrophilic treatment.

In the case that the gel forming solution is crosslinked to polymerization on the surface of the support, the surface of the gel forming solution can be covered with a cover film, sheet, or plate. The same material as employable for the support can be employed as the cover film, sheet, and plate.

A polyol compound such as glycerol or ethylene glycol can be contained in the polyacrylamide gel membrane of the element of the invention as a wetting agent. The polyol compound can be introduced in an amount of approx. 5 to 40 wt.% based on the volume of the aqueous gel membrane. Glycerol is particularly preferable among the polyol compounds. The addition of the wetting agent serves to keep the gel membrane from excessive dryness possibly caused by evaporation of water during storage of the medium, whereby preventing the medium from turning brittle or cracking caused by the excessive dryness. Thus, the improvement of physical properties of the gel membrane is accomplished.

The gel membrane of the invention can be employed for the horizontal or vertical electrophoresis, disc electrophoresis, etc. by known methods described, for instance, in the aforementioned texts.

The medium for electrophoresis provided to the element of the present invention is strongly bound to the support through the provision of the specific adhesive layer. Accordingly, the element for electrophoresis of the present invention is always kept in the form of an integrated unit in the course of ordinary operations. For this reason, the complicated operations conventionally required in the electrophoresis of proteins or conjugated proteins cay be simplified by the use of the element for electrophoresis according to the present invention. Moreover, the electrophoresis operation and dyeing operation can be performed by the integrated structure comprising the support and the gel membrane provided thereon.

The present invention will be more clearly understood with reference to the following examples.

EXAMPLE 1

The polymer set forth in Table 1 was coated on a polyethylene terephthalate (PET) sheet (i.e., support) having been made hydrophilic by irradiation of ultraviolet rays and dried to approx. 110° C. to form an adhesive layer of approx. 0.5 μm thick (solid portion).

<pre xml:space="preserve" listing-type="tabular"> <!--Greenbook tabular data--> TABLE 1______________________________________Composition of Coating Solution for theFormation of Adhesive LayerSample No. Polymer Polymer Content______________________________________1 Polyacrylamide 5 g.2 Polyacrylamide 4.5 g. BIS 0.5 g.3 P - 2 5 g.4 P - 5 5 g.5 P - 6 5 g.______________________________________</pre>

Remarks: The polymer content means that water was added to the polymer in the indicated amount to give 100 ml. of aqueous polymer solution. BIS means N,N'-methylenebisacrylamide. P-2, P-5, and P-6 means the polymers respectively illustrated hereinbefore.

The adhesiveness between the PET sheet (support) and the adhesive layer was evaluated by a cross-cut method. As a result, it was observed that the samples 3, 4 and 5 (according to the present invention) were satisfactory in the adhesiveness, while the samples 1 and 2 (control samples) showed sepration of the adhesive layer from the support in not a few portions.

On the adhesive layer provided on the support was formed a polyacrylamide gel membrane of 0.5 mm thick by coating an aqueous solution containing 9.5 g. of acrylamide, 0.5 g. of BIS, 3.58 g. of disodium hydrogenphosphate 12 hydrates, 0.33 g. of sodium dihydrogenphosphate 2 hydrates, and 0.10 g. of sodium dodecylsulfate (SDS) in 100 ml. volume after addition of 1.3 ml of ammonium peroxodisulfate (5 weight %) and 33 μl. of TEMED, both being the polymerization initiator. Thus, an element for electrophoresis was obtained.

The adhesiveness between the polyacrylamide gel membrane and the support in the element for electrophoresis was evaluated by pressing the gel membrane. As a result, it was observed that the samples 3, 4 and 5 (according to the present invention) were satisfactory in the adhesiveness, while the samples 1 and 2 (control samples) were poor in the adhesiveness.

EXAMPLE 2

The PET sheet provided with the adhesive layer was prepared in the same manner as in Example 1 using the polymer set forth in Table 1. On the adhesive layer was formed a polyacrylamide gel membrane of 0.5 mm thick by coating an aqueous solutiona containing 9.5 g. of acrylamide, 0.5 g. of BIS, 0.3 g. of agarose (low electroendomosis, gelatin temperature 36° C.), 2.5 g. of polyacrylamide, 3.58 g. of disodium hydrogenphosphate 12 hydrates, 0.33 g. of sodium dihydrogenphosphate 2 hydrates, and 0.10 g. of sodium dodecylsulfate (SDS) in 100 ml. volume after addition of 1.3 ml of ammonium fate (5 weight %) and 33 μl. of TEMED, both being the polymerization initiator. Thus, an element for electrophoresis was obtained.

A control protein was electrophoresed on the polyacrylamide gel membrane. The element was then immersed in an aqueous Coomasie Blue R-250 solution (1%) for dyeing. In this dyeing process, the adhesiveness between the support and the polyacrylamide gel membrane was observed for each element.

In the sample 1 (control sample), the gel membrane completely separated from the support immediately after the element was immersed in the dye solution. In the sample 2 (control sample), the gel membrane was bound to the support in the initial stage of the dyeing process, but separated in the end of the dyeing process.

In contrast, all of the gel membranes in the samples 3, 4, and 5 (according to the present invention) were completely bound to the support during the dyeing process. In addition, no unsatisfactory results were observed in the electrophoresis in the use of the samples 3, 4 and 5.

EXAMPLE 3

A polyacrylamide gel membrane was formed on the adhesive layer of the PET sheet to prepare an element for electrophoresis in the same manner as in Example 2. The gel membrane was cut together with the support, and the cut face (section) of the gel membrane was observed. Partial separation of the gel membrane from the support was observed in the samples 1 and 2 (control samples), while no separation was observed in the samples 3, 4 and 5 (according to the present invention). This means that the element for electrophoresis according to the invention can be cut with no unfavorable separation between the gel membrane and the support.